Malonsaeureamid-thioanilid

Base Information

Chemical Name:Malonsaeureamid-thioanilid
CAS No.:1132-43-0
Molecular Formula:C₉H₁₀N₂OS
Molecular Weight:194.257
Hs Code.:

Synonyms:Malonsaeureamid-thioanilid

Suppliers and Price of Malonsaeureamid-thioanilid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Malonsaeureamid-thioanilid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Malonsaeureamid-thioanilid

There total 2 articles about Malonsaeureamid-thioanilid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1139-69-1
2-acetyl-N¹-phenyl-thiomalonamide

: 1132-43-0
Malonsaeureamid-thioanilid

Guidance literature:: With potassium hydroxide;

Reference yield:

: 103-72-0
phenyl isothiocyanate

: 1132-43-0
Malonsaeureamid-thioanilid

Guidance literature:: Multi-step reaction with 2 steps

1: (i) KOtBu, tBuOH, THF, (ii) /BRN= 471392/

2: aq. KOH

With potassium hydroxide;

Reference yield: 70.0%

: 5660-83-3
2-cyclopentylidene malononitrile

: 1132-43-0
Malonsaeureamid-thioanilid

: 1521-51-3,113667-32-6
rac-3-bromocyclohexene

: 9-amino-7-(cyclohex-2-en-1-ylthio)-10-cyano-N-phenyl-8-azaspiro[4.5]deca-6,9-diene-6-carboxamide

Guidance literature:: 2-cyclopentylidene malononitrile; Malonsaeureamid-thioanilid; With ethanol; sodium; at 20 ℃; for 25h;

rac-3-bromocyclohexene; In ethanol; at 20 ℃; for 3h;
DOI:10.1007/s11172-021-3172-9